A system for quantification of neurite outgrowth in in-vitro
experiments is described. The system is developed for routine use
in a high-throughput setting and is therefore needs fast, cheap,
and robust. It relies on automated digital microscopical imaging
of microtiter plates. Image analysis is applied to extract
features for characterisation of neurite outgrowth. The system is
tested in a dose-response experiment on PC12 cells + Taxol. The
performance of the system and its ability to measure changes on
neuronal morphology is studied.
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